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Integrin β8 facilitates tumor growth and drug resistance through a Y‐box binding protein 1‐dependent signaling pathway in bladder cancer

机译:整合素β8通过膀胱癌中的Y盒结合蛋白1依赖信途径促进肿瘤生长和耐药性

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摘要

The transmembrane receptors integrins are the bridges for cell‐cell or cell‐ECM interaction, which is strictly correlated to cancer development in several tumor types. Here, we revealed that integrin β8 serves as a driver to mediate sustained growth of bladder cancer and development of drug resistance. The elevated expression of integrin β8 was observed in highly malignant bladder tumor tissues from patients. The in vitro and in vivo results further indicated that integrin β8 overexpression in Biu87/T24 bladder cancer could mediate and strengthen cell proliferation and resistance to mitomycin C and hydroxycamptothecin. Mechanistically, integrin β8 on the cellular surface might recruit phosphorylated Y‐box binding protein 1, leading to the activation of c‐Myc and nuclear factor‐κB signals. Pharmacological targeting of integrin β8 by Arg‐Gly‐Asp‐Ser efficiently suppressed sustained growth and drug resistance in bladder cancer cells. Our findings identified integrin β8 as a marker of bladder cancer diagnosis and development, and provides an innovative approach for clinical bladder cancer therapy.
机译:跨膜受体整合素是用于细胞 - 细胞或细胞-ECM相互作用的桥梁,其与几种肿瘤类型中的癌症发育严格相关。在这里,我们透露,整合素β8用作助长膀胱癌的持续增长和耐药性的驾驶员。从患者的高度恶性膀胱肿瘤组织中观察到整合蛋白β8的升高表达。体外和体内的结果进一步表明,BIU87 / T24膀胱癌中的整联蛋白β8过表达可以介导和加强细胞增殖和对丝霉素C和羟基清除素的抗性。机械地,细胞表面上的整联蛋白β8可以募集磷酸化的Y盒结合蛋白1,导致C-MYC和核因子-κB信号的激活。通过Arg-Gly-ASP-SER有效地抑制膀胱癌细胞中持续增长和耐药性的药理学靶向。我们的研究结果将整合蛋白β8作为膀胱癌诊断和开发的标志物,为临床膀胱癌治疗提供了一种创新方法。

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